FDA-Registered & Audit-Ready
Production runs under 21 CFR Part 111 and Part 117 with SQF Edition 9 and GMP certification. Batch records, allergen controls and retained samples are documented for retailer and marketplace audits.
Springville, Utah · FDA-Registered Facility
From Concept to Market-Ready in 90 Days
US-based supplement contract manufacturing across six dosage forms — gummies, powders, tablets, softgels, hard capsules and pet nutrition. Built for brands that need speed without compromising compliance.
21 CFR 111 & 117 Compliant GMP & SQF Edition 9 Halal & Kosher Available
Manufacturing Capability Snapshot
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Days from brief to market-ready batch
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Formulations delivered to North American brands
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In-house dosage form platforms
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Manufacturing regions: USA · EU · China
FDA-registered production under dietary supplement cGMP
Certificate of Analysis & full batch records on every run
30 years of global CDMO manufacturing heritage
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Concept to Market-Ready
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Formulations Delivered
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On-Time Batch Release Rate
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Years Global CDMO Experience
FDA-Registered Manufacturing GMP & SQF Certified 8–12 Week Lead Times USA · EU · China Network Halal & Kosher Options
Why Brands Choose PAG USA
The supplement manufacturing partner built around your launch date
We are a contract development and manufacturing organization (CDMO), not a broker. Formulation, blending, encapsulation, deposit, packaging and release testing all happen inside facilities we operate and audit — which is why our timelines hold.
90-Day Launch Discipline
Private label programs ship in 8–10 weeks; full custom formulation runs 12–16 weeks including accelerated stability. One project manager owns your timeline from brief to pallet.
MOQs Sized for Growth
Start at 6,000 units for gummies, 5,000 units for tablets, softgels and capsules, or 300 kg for powders — then scale to multi-container volumes on the same equipment and specifications.
Global Integrated System
Utah for US demand, an EU-GMP plant in the Netherlands for Europe, and Shenzhen for volume and raw material sourcing — one specification set across three continents.
What We Manufacture
Six Dosage Forms. One Accountable Partner.
Every format below is produced in our US FDA-registered, GMP-certified facility with in-process quality checks and a Certificate of Analysis on each production run.
Gummies
From 6,000 units
Pectin or gelatin base, sugar-free options, custom molds, flavors and colors with validated active recovery.
Gummy manufacturing →
Powders
From 300 kg
Bulk jars, sachets and stick packs for pre-workout, protein, greens, collagen and electrolyte blends.
Powder manufacturing →
Tablets
From 5,000 units
Compressed, film-coated, bilayer, chewable and effervescent tablets with disintegration verification.
Tablet manufacturing →
Softgels
From 5,000 units
Oil-based actives including omega-3, CoQ10, MCT and vitamin D, with nitrogen-flushed fill protection.
Softgel manufacturing →
Hard Capsules
From 5,000 units
HPMC vegetable or bovine gelatin shells in sizes 0, 00, 000, 00E and 000E, including botanical blends.
Capsule manufacturing →
Pet Nutrition
300 kg / 2,000 units
Soft chews, pastes and powders for dogs and cats with AAFCO labeling and palatability support.
Pet nutrition →Where our client brands sell
Our Manufacturing Process
Formula to shelf in 90 days — and the data to prove it.
Most launch delays are not production problems; they are hand-off problems. We compress development, testing, production and release into one governed workflow with a single point of contact.
01
Formulation & Prototyping
Our R&D team builds your prototype in 2–3 weeks based on target claims, label panel, dosing and cost per serving.
02
Stability & Analytical Testing
Accelerated stability, microbial screening, heavy metals and potency verification through ISO-accredited laboratories.
03
cGMP Production Run
Scale-up with documented in-process controls at weighing, blending, forming, drying and primary packaging stages.
04
QA Release & Fulfillment
Certificate of Analysis, batch records and compliance documentation issued before direct-to-3PL or warehouse delivery.
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On-time batch release rate across 2024–2025 production
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Typical turnaround for a costed formulation and sample plan
0K+
Entry-level minimum order — accessible for first production runs
Who We Serve
Manufacturing programs for brands that move fast
From a first 5,000-unit Amazon SKU to a multi-region rollout, our commercial and technical teams work the same way: transparent specifications, documented quality, predictable dates.
Amazon & DTC Sellers
Private label ready with low MOQs, marketplace-compliant labeling support, Supplement Facts review and a 90-day launch cadence that matches ad-spend planning.
Most RequestedEstablished Supplement Brands
Custom formulation from a blank page, reformulation for cost or clean-label goals, or toll manufacturing of your existing validated formula with full technology transfer.
Custom Formulation & TollInternational Brands Entering the USA
Domestic production removes tariff and lead-time exposure. We handle US label conversion, FDA facility registration alignment and direct-to-3PL distribution.
US Market Entry Inside Our Facility
A look inside our US-based manufacturing plant
Controlled-environment production suites, an on-site quality laboratory, encapsulation and deposit lines, and climate-monitored warehousing — all under one roof in Springville, Utah. Facility audits are welcomed during supplier qualification.
Production Suite
Automated Lines
Warehousing
QC Laboratory
Encapsulation6
Dosage form platforms inside one FDA-registered facility — no outsourced hand-offs between formats.
View All Dosage Forms Global Integrated System Learn About Our Company
One partner. Three continents.
PAG's Global Integrated System links manufacturing in the United States, Europe and China — giving your brand scale, supply redundancy and the regulatory documentation needed to expand into new markets without re-qualifying a new supplier.
Springville, Utah — US Headquarters
FDA-registered, GMP and SQF-certified production. The primary base for North American brands: domestic lead times, no tariff exposure and a documented 90-day launch path.
Your Primary PartnerNetherlands — EU-GMP Facility
Group-owned and fully operational. EU-compliant production with Novel Food and EFSA-aligned documentation support for European market entry.
European ManufacturingShenzhen, China — Scale & Sourcing
Our Shenzhen site enters production in 2026, adding high-volume capacity, raw material sourcing leverage and R&D depth backed by 30 years of manufacturing heritage.
Scale & Volume Buyer Questions, Answered
Supplement contract manufacturing FAQs
The questions our sourcing and procurement contacts ask most often before a first production run.
MOQs start at 6,000 units for gummies, 5,000 units for tablets, softgels and hard capsules, and 300 kg for powders and stick packs. Pet nutrition begins at 300 kg for powders or 2,000 units for soft chews. These volumes are deliberately accessible so emerging DTC and marketplace brands can validate a SKU before committing to scale.
A private label program built on an existing base formula typically ships in 8 to 10 weeks. A fully custom formulation — including R&D, flavor and texture work, accelerated stability testing and the first production run — takes 12 to 16 weeks. That is how we deliver a market-ready finished product inside our 90-day commitment.
Manufacturing takes place in an FDA-registered facility operating under 21 CFR Part 111 (dietary supplement cGMP) and 21 CFR Part 117 (preventive controls for human food), with GMP and SQF Edition 9 certification. Halal, Kosher and USDA Organic handling programs are available on request. Certificate copies are shared under NDA during supplier qualification. FDA registration does not constitute FDA approval or endorsement of any product.
Each batch is released with a Certificate of Analysis covering identity, potency, heavy metals and microbiology, plus batch production records, raw material specifications, allergen statements and retained samples. The documentation package is structured to satisfy marketplace compliance reviews, retailer onboarding and third-party audits.
Yes. We routinely accept technology transfers of validated formulas. Our team reviews the bill of materials, sources or qualifies equivalent raw materials, runs a pilot batch for comparability, and documents the process so your finished product remains consistent with prior production while gaining our US capacity and lead times.
We handle primary and secondary packaging — bottles, pouches, stick packs, jars, blisters and unit cartons — including induction sealing, lot coding and shrink banding. Label artwork is reviewed for Supplement Facts formatting and claim structure, and finished pallets ship directly to your 3PL, Amazon fulfillment center or brand warehouse.
Ready to build your supplement in the USA?
Share your formula, target market and launch date. Our Utah-based technical team replies within one business day, Monday to Friday, 9:00am–6:00pm Mountain Time.
FDA registration does not constitute FDA approval or endorsement of any product. Certifications are held by our FDA-registered manufacturing operation; certificate copies are available under NDA during supplier qualification.